It is indispensable to mention that the pharmaceutical industry is paramount to developing public health policies. It is essential to protect the safety and quality of medicines. This is where WHO GMP Certification comes into play. A WHO GMP Certified Third Party Manufacturer maintains a high level of compliance with international production standards. Several measures need to be implemented regarding these standards to enhance the medicines’ safety, quality and efficacy.
Today’s blog will discuss WHO GMP compliance, how to proceed with WHO GMP. Additionally, here we will explain the significance of selecting a WHO GMP certified pharmaceutical company.
What is WHO-GMP Certification in the Indian Pharmaceutical Industry?
WHO means “World Health Organization” and GMP is abbreviated as “Good Manufacturing Practices”. It is a group of measures guaranteeing that medicines are made and checked consistently. Being a WHO GMP certified company in India, they practice systematic guidelines that may encompass every aspect of business, from the procurement of raw materials to the distribution of products.
Click Here to Get Best Manufacturing Quote
These guidelines help to avoid dangers such as contamination, mistakes, and product inconsistency. In turn, they guarantee the protection and efficiency of medicines. In terms of global competitiveness, a WHO GMP certified third party manufacturer means that a business needs a reliable product provider to solve its healthcare needs.
Is it Mandatory to have WHO GMP Certificate for Pharma Companies?
WHO-GMP certification is not legally mandatory in all countries around the globe. However, it is highly recommended and often necessary for exporting medicines. Some world markets, especially those in Europe and the US, require products from their source country to be certified for export.
In India, getting a WHO-GMP certificate means something and makes everyone believe in you. This makes companies competitive internationally since they want to meet the specified standards. Hence, becoming the WHO GMP certified third party manufacturer gives aesthetic access to the global market and customer loyalty.
Process of Applying for the WHO-GMP Certification in India
The process of getting WHO-GMP certification is not a complex one but can take quite some time. Here’s an overview of the process:
- Preparation: Make sure that this facility complies with the GMP regulations. This comprises hygiene, equipment, and the people who are trained to handle this equipment.
- Application Submission: Form the application with the required documents as per the regulatory authority’s requirements.
- Inspection: Legal entities carry out thorough investigations of the facility. They also monitor compliance with WHO-GMP requirements.
- Report Analysis: The inspection report is shared and reviewed by relevant authorities. If there is any non-compliance, all those issues must be addressed.
- Certification: After fulfilling all the requirements, the company gets the required WHO-GMP certification.
Such a process helps a WHO-GMP certified pharmaceutical company to sustain high-quality standards.
Benefits of Connecting with a WHO GMP Certified Third Party Manufacturer in India
Outsourcing pharma manufacturing requirements to third-party companies exhibits several benefits to the pharma owners. This includes:
Firstly, it guarantees quality in products that are within the reach of consumers. Manufacturers follow certain procedures that help them reduce possible risks and keep their products safe for use.
Click Here to Get Best Manufacturing Quote
Secondly, outsourcing production to certified manufacturers is less pricing as comparative to setup own manufacturing unit. Many organizations can reduce infrastructure, labor, and equipment costs significantly.
Furthermore, the leading WHO-GMP certified third party manufacturer undertakes legal requirements responsibilities. This means that pharmaceutical firms can concentrate on promoting and supplying their products.
Moreover, there is an experienced WHO-GMP certified pharmaceutical company in India with the added advantage of scale-up. It can quickly raise its production potential through fluctuations in market needs.
Join Top WHO-GMP Certified Pharmaceutical Companies in India
Taksa Pharmaceuticals, a part of Taksa Life Sciences, operates in Dera Bassi, Mohali, Punjab, and is one of the distinguished WHO-ISO-GMP-certified pharmaceutical companies in India. Established in 2006, they deal in third-party manufacturing and deals in more than 350 neurological disorder medicines. Their contemporary manufacturing facility responds to WHO-GMP regulations concerning producing high-quality products within different therapeutic categories.
Along with it, their distribution channel ensures that Taksa Pharma delivers affordable healthcare products nationwide within the shortest time possible. Their pledges to quality, customer care, and attainment of same-day dispatch services make them ideal partners in the pharma manufacturing industry.
So, if you are seeking to have WHO-GMP certification for your organization or if you’re searching for a reliable WHO-GMP certified third party manufacturer in your region then Taksa Pharma will be your best guide.
Frequently Asked Questions
2. Why is this WHO GMP certification necessary?
The GMP-WHO-certification for pharmaceutical company strengthens their organization’s reliability. Along with it, it guarantees that they follow the rules and open doors to overseas operations.
3. How can I connect with a Reliable WHO GMP Certified Third Party Manufacturer?
In this digital era, you can simply visit their website or you can find their customer’s feedback over Google. Another way is to find their contact details in pharmaceutical directories.
Contact Taksa Pharma:
Admin Office: Plot No: 124, #101, Sector 45-B, Chandigarh – 160047 (India)
Email Address: taksapharmaceuticals@gmail.com
Mobile Number: +91-8146567358
